Run ID: SRR6257065
Sample name:
Date: 04-04-2023 13:25:01
Number of reads: 354543
Percentage reads mapped: 98.44
Strain: lineage2.2.1
Drug-resistance: HR-TB
Drug | Resistance | Supporting mutations |
---|
Lineage | Family | Main Spoligotype | RDs | Frequency |
---|---|---|---|---|
lineage2 | East-Asian | Beijing | RD105 | 1.0 |
lineage2.2 | East-Asian (Beijing) | Beijing-RD207 | RD105;RD207 | 1.0 |
lineage2.2.1 | East-Asian (Beijing) | Beijing-RD181 | RD105;RD207;RD181 | 1.0 |
Gene | Chromosome position | Mutation | Type | Estimated fraction | Drugs |
---|---|---|---|---|---|
rpsL | 781687 | p.Lys43Arg | missense_variant | 1.0 | streptomycin |
katG | 2155168 | p.Ser315Thr | missense_variant | 1.0 | isoniazid |
Gene | Chromosome position | Mutation | Type | Estimated fraction |
---|---|---|---|---|
gyrA | 6922 | c.-380G>T | upstream_gene_variant | 0.25 |
gyrA | 7362 | p.Glu21Gln | missense_variant | 1.0 |
gyrA | 7585 | p.Ser95Thr | missense_variant | 1.0 |
gyrA | 9290 | c.1989G>T | synonymous_variant | 0.4 |
gyrA | 9304 | p.Gly668Asp | missense_variant | 1.0 |
gyrA | 9333 | p.Gly678Trp | missense_variant | 0.29 |
fgd1 | 491355 | c.573C>A | synonymous_variant | 0.5 |
fgd1 | 491742 | c.960T>C | synonymous_variant | 1.0 |
mshA | 575416 | c.69T>C | synonymous_variant | 0.18 |
mshA | 575907 | p.Ala187Val | missense_variant | 1.0 |
ccsA | 620620 | p.Val244Met | missense_variant | 0.17 |
ccsA | 620625 | p.Ile245Met | missense_variant | 1.0 |
rpoB | 761943 | c.2137C>T | synonymous_variant | 0.29 |
rpoC | 763031 | c.-339T>C | upstream_gene_variant | 1.0 |
rpoC | 763301 | c.-69C>G | upstream_gene_variant | 0.2 |
rpoC | 765244 | c.1875T>A | synonymous_variant | 0.29 |
rpoC | 766645 | p.Glu1092Asp | missense_variant | 1.0 |
mmpL5 | 775639 | p.Ile948Val | missense_variant | 1.0 |
mmpL5 | 775712 | c.2769G>A | synonymous_variant | 0.2 |
mmpL5 | 775826 | c.2655G>A | synonymous_variant | 0.2 |
mmpL5 | 775871 | c.2610C>T | synonymous_variant | 0.22 |
mmpL5 | 775874 | c.2607C>A | synonymous_variant | 0.22 |
mmpL5 | 776003 | c.2478C>T | synonymous_variant | 0.18 |
mmpL5 | 776008 | p.His825Asp | missense_variant | 0.17 |
mmpL5 | 776009 | c.2472A>G | synonymous_variant | 0.17 |
mmpL5 | 776100 | p.Thr794Ile | missense_variant | 1.0 |
mmpL5 | 776182 | p.Asp767Asn | missense_variant | 1.0 |
mmpL5 | 776670 | p.Phe604Ser | missense_variant | 0.11 |
mmpL5 | 777563 | c.918C>T | synonymous_variant | 0.22 |
mmpR5 | 779062 | p.Gly25Cys | missense_variant | 0.33 |
mmpS5 | 779615 | c.-710C>G | upstream_gene_variant | 1.0 |
rpsL | 781395 | c.-165T>C | upstream_gene_variant | 1.0 |
fbiC | 1303016 | p.Val29Gly | missense_variant | 0.33 |
fbiC | 1305038 | p.Arg703Leu | missense_variant | 0.17 |
Rv1258c | 1406760 | c.580_581insC | frameshift_variant | 1.0 |
rrs | 1471659 | n.-187C>T | upstream_gene_variant | 1.0 |
rrs | 1473221 | n.1376C>A | non_coding_transcript_exon_variant | 0.14 |
rrl | 1473722 | n.65G>C | non_coding_transcript_exon_variant | 0.15 |
rrl | 1473727 | n.70G>A | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475024 | n.1367G>T | non_coding_transcript_exon_variant | 0.15 |
rrl | 1475187 | n.1530C>A | non_coding_transcript_exon_variant | 0.13 |
fabG1 | 1673380 | c.-60C>G | upstream_gene_variant | 0.36 |
fabG1 | 1673899 | p.Ala154Ser | missense_variant | 0.29 |
inhA | 1674376 | p.Pro59Ala | missense_variant | 0.25 |
inhA | 1674567 | c.366C>A | synonymous_variant | 0.2 |
rpsA | 1833388 | c.-154C>A | upstream_gene_variant | 0.25 |
rpsA | 1834177 | c.636A>C | synonymous_variant | 1.0 |
rpsA | 1834610 | p.Arg357Trp | missense_variant | 0.18 |
tlyA | 1917972 | c.33A>G | synonymous_variant | 1.0 |
tlyA | 1917981 | c.42G>C | synonymous_variant | 0.25 |
ndh | 2103120 | c.-78C>A | upstream_gene_variant | 0.12 |
katG | 2154724 | p.Arg463Leu | missense_variant | 1.0 |
katG | 2155578 | c.534C>T | synonymous_variant | 0.13 |
PPE35 | 2167814 | c.2799C>T | synonymous_variant | 0.15 |
PPE35 | 2167865 | c.2748G>C | synonymous_variant | 0.12 |
PPE35 | 2167868 | c.2745A>C | synonymous_variant | 0.12 |
PPE35 | 2167926 | p.Leu896Ser | missense_variant | 1.0 |
PPE35 | 2167931 | c.2682C>T | synonymous_variant | 0.12 |
PPE35 | 2167936 | p.Thr893Ala | missense_variant | 0.11 |
PPE35 | 2167937 | c.2676A>C | synonymous_variant | 0.11 |
PPE35 | 2169287 | c.1326T>C | synonymous_variant | 0.15 |
PPE35 | 2169779 | c.834A>C | synonymous_variant | 0.15 |
PPE35 | 2169831 | p.Asn261Ile | missense_variant | 0.17 |
PPE35 | 2170048 | p.Leu189Val | missense_variant | 0.33 |
PPE35 | 2170053 | p.Thr187Ser | missense_variant | 0.33 |
PPE35 | 2170187 | c.426G>A | synonymous_variant | 0.13 |
PPE35 | 2170193 | p.Tyr140* | stop_gained | 0.12 |
PPE35 | 2170544 | c.69G>A | synonymous_variant | 0.13 |
PPE35 | 2170547 | c.66A>C | synonymous_variant | 0.14 |
Rv1979c | 2223293 | c.-129A>G | upstream_gene_variant | 1.0 |
pncA | 2289367 | c.-126C>A | upstream_gene_variant | 0.14 |
kasA | 2518864 | c.750G>C | synonymous_variant | 0.15 |
kasA | 2518879 | c.765A>G | synonymous_variant | 0.13 |
kasA | 2518882 | c.768C>A | synonymous_variant | 0.13 |
kasA | 2519128 | c.1014G>C | synonymous_variant | 0.2 |
kasA | 2519131 | c.1017G>C | synonymous_variant | 0.22 |
eis | 2714278 | p.Asp352Gly | missense_variant | 0.17 |
eis | 2715068 | p.Pro89Thr | missense_variant | 0.14 |
eis | 2715540 | c.-208C>T | upstream_gene_variant | 0.4 |
ahpC | 2726335 | p.Arg48Leu | missense_variant | 0.14 |
folC | 2746318 | c.1281C>A | synonymous_variant | 0.15 |
ribD | 2986928 | p.Gln30His | missense_variant | 0.33 |
ribD | 2987173 | p.Ser112Asn | missense_variant | 0.33 |
Rv2752c | 3064949 | p.Val415Ile | missense_variant | 0.14 |
Rv2752c | 3065480 | p.Phe238Leu | missense_variant | 0.22 |
ald | 3086788 | c.-32T>C | upstream_gene_variant | 1.0 |
fbiD | 3339442 | p.Asn109Asp | missense_variant | 0.14 |
fbiD | 3339547 | p.Leu144Phe | missense_variant | 0.25 |
fprA | 3473996 | c.-11_-10insA | upstream_gene_variant | 1.0 |
whiB7 | 3568577 | p.Gly35Cys | missense_variant | 0.17 |
Rv3236c | 3612149 | p.Gln323Arg | missense_variant | 0.12 |
Rv3236c | 3612282 | p.Gly279Ser | missense_variant | 0.14 |
Rv3236c | 3612289 | c.828G>T | synonymous_variant | 0.17 |
Rv3236c | 3612813 | p.Thr102Ala | missense_variant | 1.0 |
fbiB | 3641609 | c.75C>A | synonymous_variant | 0.15 |
fbiB | 3641647 | p.Pro38Gln | missense_variant | 0.17 |
fbiB | 3642415 | p.Pro294Leu | missense_variant | 0.17 |
alr | 3840691 | p.Pro244Thr | missense_variant | 0.2 |
alr | 3841018 | c.403C>T | synonymous_variant | 0.22 |
alr | 3841612 | c.-193_-192insC | upstream_gene_variant | 0.16 |
rpoA | 3877769 | p.Phe247Leu | missense_variant | 0.4 |
ddn | 3987030 | p.Pro63Thr | missense_variant | 0.14 |
clpC1 | 4039003 | p.Asn568Asp | missense_variant | 0.16 |
clpC1 | 4039498 | p.Ile403Val | missense_variant | 0.18 |
clpC1 | 4039682 | c.1023C>T | synonymous_variant | 0.14 |
clpC1 | 4040144 | c.561G>C | synonymous_variant | 0.18 |
embC | 4239834 | c.-29G>T | upstream_gene_variant | 0.14 |
embA | 4242643 | c.-590C>T | upstream_gene_variant | 1.0 |
embA | 4243460 | c.228C>T | synonymous_variant | 1.0 |
embA | 4244208 | p.Leu326Met | missense_variant | 0.5 |
embA | 4244219 | c.987C>A | synonymous_variant | 0.5 |
embA | 4245081 | p.Ala617Thr | missense_variant | 0.4 |
embA | 4246449 | p.Val1073Phe | missense_variant | 0.13 |
embB | 4247375 | p.Leu288Met | missense_variant | 0.15 |
embB | 4249022 | p.Leu837Ile | missense_variant | 0.33 |
aftB | 4267103 | c.1734G>T | synonymous_variant | 0.22 |
aftB | 4267647 | p.Asp397Gly | missense_variant | 1.0 |
aftB | 4267708 | p.Gly377Trp | missense_variant | 0.22 |
aftB | 4268283 | p.Val185Ala | missense_variant | 0.15 |
ubiA | 4269566 | p.Arg90Trp | missense_variant | 0.33 |
ethA | 4327235 | p.Pro80His | missense_variant | 0.2 |
ethR | 4327432 | c.-117G>A | upstream_gene_variant | 0.22 |
ethR | 4327961 | p.Trp138Leu | missense_variant | 0.2 |
whiB6 | 4338595 | c.-75delG | upstream_gene_variant | 1.0 |
whiB6 | 4338685 | c.-164C>A | upstream_gene_variant | 0.17 |
gid | 4407588 | c.615A>G | synonymous_variant | 1.0 |
gid | 4407927 | p.Glu92Asp | missense_variant | 1.0 |